BD PERSIST- povidone-iodine, alcohol solution

BD PERSIST by

Drug Labeling and Warnings

BD PERSIST by is a Otc medication manufactured, distributed, or labeled by Becton Dickinson and Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Providone-Iodine 10% (w/w)

Ethyl Alcohol 70% (v/v)

Purpose

Antiseptic

Antiseptic

Uses

• for preparation of the skin prior to percutaneous procedure
• helps reduce bacteria that potentially can cause skin infection
• does not contribute to skin irritation under an occlusive dressing with repeated applications
• reduces bacteria with routine site care for up to seven days

Warnings

• For external use only
• contains alcohol which is flammable until dry
• Single use only

Do not use

• if you are allergic to povidone iodine or ethyl alcohol
• to treat wounds or burns
• in eyes, mucus membranes
• on broken skin
• with electrocautery procedures

Stop use and ask a doctor if the insertion site becomes

• red
• irritated
• swollen
• painful
• infected

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply with friction for 30 seconds
• allow to dry
• do not blot or wipe away

Inactive ingredients

acrylates copolymer, ethyl alcohol, isopropyl myristate, urea, water

PRINCIPAL DISPLAY PANEL

Principal Display Panel – Carton Label

BD Persist™
Skin Prep

One Step Application
One Swab Stick
Non-sterile solution

50

PRINCIPAL DISPLAY PANEL

Principal Display Panel – Package Label

BD Persist™ Skin Prep
1 Swab Stick Non-sterile solution REF 386401 NDC: 17271-507-01

INGREDIENTS AND APPEARANCE

BD PERSIST 
povidone-iodine, alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17271-507
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
povidone-iodine (UNII: 85H0HZU99M) (iodine - UNII:9679TC07X4)	iodine	85 mg  in 1 mL
alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M)	alcohol	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
carbomer copolymer Type A (UNII: 71DD5V995L)
ethyl acetate (UNII: 76845O8NMZ)
isopropyl myristate (UNII: 0RE8K4LNJS)
urea (UNII: 8W8T17847W)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17271-507-01	50 in 1 CARTON	02/21/1996
1		2 mL in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 17271-507-02	25 in 1 CARTON	02/21/1996
2		7 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/21/1996

Labeler - Becton, Dickinson and Company (124987988)

Establishment
Name	Address	ID/FEI	Business Operations
Becton, Dickinson and Company		124987988	MANUFACTURE(17271-507)